A concurrently optimization of H and OH binding energies in atomically Ni anchored Ru/RuO2 nanosheet driving high CO-tolerant hydrogen oxidation catalysis

The development of highly active and CO-tolerant hydrogen oxidation reaction (HOR) electrocatalysts is of great significance for alkaline exchange membrane fuel cells (AEMFCs). Here, the designed atomically Ni anchored Ru/RuO<sub>2</sub> heterostructure nanosheets (Ni<sub>SA</sub>-Ru@RuO<sub>2</sub> NSs/C) exhibit enhanced activity and stability for HOR in alkaline media. The optimized electrocatalyst delivers a high CO-tolerant durability with 92.3% retention in the 1000 ppm CO concentration after 5000 s test. Moreover, the anode catalyst Ni<sub>SA</sub>-Ru@RuO<sub>2</sub> NSs/C assembled AEMFCs output a peak power density (PPD) and specific PPD of 1.76 W cm<sup>-2</sup> and 17.6 W mg<sub>PGM</sub><sup>-1</sup> under the H<sub>2</sub>/O<sub>2</sub> condition and performed a long-term stability with negligible decay for 100 h at 0.5 A cm<sup>-2</sup> for the AEMFCs. The relative mechanism studies reveal that the Ru/RuO<sub>2</sub> heterostructure nanosheet and dispersed Ni single atoms have optimized the *H and *OH adsorption simultaneously and weaken the *CO adsorption. Our work may offer a significant guideline on the rational design of high-performance HOR electrocatalyst for energy-related applications.

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Publication Details

Journal
Nature Communications
Published
2025-10-08
DOI
https://doi.org/10.1038/s41467-025-63998-8
Citations
3
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
1.55

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article

A concurrently optimization of H and OH binding energies in atomically Ni anchored Ru/RuO2 nanosheet driving high CO-tolerant hydrogen oxidation catalysis

Zhiwei Hu, Nan Fang, Renjie Ren, Lin Zhuang et al.
3 citations
Nature Communications
Catalytic Processes in Materials Science
1.55
article

A concurrently optimization of H and OH binding energies in atomically Ni anchored Ru/RuO2 nanosheet driving high CO-tolerant hydrogen oxidation catalysis

Zhiwei Hu, Nan Fang, Renjie Ren, Lin Zhuang, Youyong Li, Qi Shao, Yujin Ji, Xiaoqing Huang, Qingyu Kong, Lujie Jin, Liangbin Liu, Wei Yan
article en
3 citations

Abstract

The development of highly active and CO-tolerant hydrogen oxidation reaction (HOR) electrocatalysts is of great significance for alkaline exchange membrane fuel cells (AEMFCs). Here, the designed atomically Ni anchored Ru/RuO<sub>2</sub> heterostructure nanosheets (Ni<sub>SA</sub>-Ru@RuO<sub>2</sub> NSs/C) exhibit enhanced activity and stability for HOR in alkaline media. The optimized electrocatalyst delivers a high CO-tolerant durability with 92.3% retention in the 1000 ppm CO concentration after 5000 s test. Moreover, the anode catalyst Ni<sub>SA</sub>-Ru@RuO<sub>2</sub> NSs/C assembled AEMFCs output a peak power density (PPD) and specific PPD of 1.76 W cm<sup>-2</sup> and 17.6 W mg<sub>PGM</sub><sup>-1</sup> under the H<sub>2</sub>/O<sub>2</sub> condition and performed a long-term stability with negligible decay for 100 h at 0.5 A cm<sup>-2</sup> for the AEMFCs. The relative mechanism studies reveal that the Ru/RuO<sub>2</sub> heterostructure nanosheet and dispersed Ni single atoms have optimized the *H and *OH adsorption simultaneously and weaken the *CO adsorption. Our work may offer a significant guideline on the rational design of high-performance HOR electrocatalyst for energy-related applications.

Nature CommunicationsVol. 16(1)
Xiamen University (CN), Synchrotron soleil (FR), Wuhan University (CN), Soochow University (CN), Max Planck Institute for Chemical Physics of Solids (DE), Tan Kah Kee Innovation Laboratory (CN)
National Natural Science Foundation of China, Xiamen University, Priority Academic Program Development of Jiangsu Higher Education Institutions, Collaborative Innovation Center of Suzhou Nano Science and Technology, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 16%
Catalytic Processes in Materials Science
1.55
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